Excited State Process of a Novel NIR-BODI Molecule in Toluene and Acetonitrile Solvents: A Theoretical Study

Excited State Process of a Novel NIR-BODI Molecule in Toluene and Acetonitrile Solvents: A Theoretical Study

Year:    2017

Journal of Atomic and Molecular Sciences, Vol. 8 (2017), Iss. 4 : pp. 162–168

Abstract

In this work, using DFT and TDDFT methods, we investigated the excited-state intramolecular proton transfer (ESIPT) mechanism of a novel NIR-BODI system [Org Biomol Chem 15:4072, 2017.] in both toluene and acetonitrile $({\rm CH}_3{\rm CN})$ solvents theoretically. Comparing the prime structural variations of NIR-BODI involved in the intramolecular hydrogen bond, we can conclude that O-H∙∙∙N should be strengthened in the $S_1$ state, which may facilitate the ESIPT process. Concomitantly, infrared vibrational spectra analysis further verify the stability of hydrogen bond. In good agreement with previous experimental results, NIR-BODI reveals two kinds of excited-state structures (NIR-BODI-enol* and NIR-BODI-keto*). Analysis about charge redistribution reveals the tendency of ESIPT process. Our scanned potential energy curves according to variational O-H coordinate demonstrates that the proton transfer process should be more likely to occur in the $S_1$ state due to the inappreciable potential energy barriers. In addition, due to the minute differences of potential energy curves contrasting toluene (the NIR-BODI-keto could be not located) and ${\rm CH}_3{\rm CN}$ (the NIR-BODI-keto can be located) solvents in $S_0$ state, we deem that solvent effect could play roles NIR-BODI system. Given the $S_1$-state potential energy barriers, we confirm that the ESIPT process is easier in ${\rm CH}_3{\rm CN}$ solvent.

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Journal Article Details

Publisher Name:    Global Science Press

Language:    English

DOI:    https://doi.org/10.4208/jams.102617.120817a

Journal of Atomic and Molecular Sciences, Vol. 8 (2017), Iss. 4 : pp. 162–168

Published online:    2017-01

AMS Subject Headings:    Global Science Press

Copyright:    COPYRIGHT: © Global Science Press

Pages:    7

Keywords: